European Conference on

Drug Discovery

June 23-24, 2025
Mercure Hotel MOA Berlin, Berlin, Germany
Home > Call For Paper > Clinical Development

Clinical Development

 Objective: Prepare and submit regulatory applications to health authorities for drug approval.

 Activities: Compile comprehensive data packages from preclinical and clinical studies. Address regulatory requirements, including safety, efficacy, manufacturing processes, and labeling. Interact with regulatory agencies (e.g.,   FDA, EMA) to facilitate approval processes

 

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